Clinical Trial Assistant 1 - Sponsor dedicated - Netanya (Clinical Research)

Location: Netanya, Israel

Company

A global provider of clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.

What you will do

• Maintain clinical documents and systems, including the Trial Master File, to track site compliance and performance within project timelines.
• Prepare, distribute, file, and archive clinical documentation and reports according to standard operating procedures.
• Review study files for completeness and support the tracking of Case Report Forms, queries, and clinical data flow.
• Prepare and track clinical trial supplies and maintain related records.
• Coordinate designated project communications and documentation as a central contact for the clinical team.
• Accompany Clinical Research Associates on site visits and assist with monitoring duties after completing required training.

Requirements

• High school diploma or equivalent, with three years of administrative support experience or an equivalent combination of education, training, and experience.
• Working knowledge of Microsoft Word, Excel, and PowerPoint.
• Good written and verbal English and Hebrew communication skills.
• Effective time management, organizational skills, and the ability to maintain productive relationships with coworkers, managers, and clients.
• Awareness of Good Clinical Practice and International Conference on Harmonization guidelines, plus knowledge of applicable protocol requirements through company training.

Culture & Benefits

• Full-time employment.
• Collaboration with Clinical Research Associates and Regulatory and Start-Up teams.
• Training is provided on applicable clinical research regulatory and protocol requirements.